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rs794727421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TATC;TATC) 0 common in clinvar
Make rs794727421(-;-)
Make rs794727421(-;TATC)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position32454765
GeneDMD
is asnp
is mentioned by
dbSNPrs794727421
dbSNP (old)rs794727421
ClinGenrs794727421
ebirs794727421
HLIrs794727421
Exacrs794727421
Varsomers794727421
Maprs794727421
PheGenIrs794727421
Biobankrs794727421
1000 genomesrs794727421
hgdprs794727421
ensemblrs794727421
gopubmedrs794727421
geneviewrs794727421
scholarrs794727421
googlers794727421
pharmgkbrs794727421
gwascentralrs794727421
openSNPrs794727421
23andMers794727421
23andMe allrs794727421
SNP Nexus

SNPshotrs794727421
SNPdbers794727421
MSV3drs794727421
GWAS Ctlgrs794727421
Max Magnitude0
ClinVar
Risk rs794727421(-;-)
Alt rs794727421(-;-)
Reference Rs794727421(TATC;TATC)
Significance Pathogenic
Disease Duchenne muscular dystrophy Becker muscular dystrophy
Variation info
Gene DMD
CLNDBN Duchenne muscular dystrophy Becker muscular dystrophy
Reversed 1
HGVS NC_000023.10:g.32472882_32472885delGATA
CLNSRC
CLNACC RCV000176658.1, RCV000176659.1,